Pearson eText Organic Chemistry -- Instant Access (Pearson+)

8th Edition

ISBN: 9780135213711

Author: Paula Bruice

Publisher: PEARSON+

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Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and…

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic…

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction…

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Textbook Question

Chapter 11, Problem 44P

Bombykol is the sex pheromone of the silk moth.

Chapter 11, Problem 44P, Bombykol is the sex pheromone of the silk moth. Show how bombykol can be synthesized from the , example 1

Show how bombykol can be synthesized from the following compounds.

Chapter 11, Problem 44P, Bombykol is the sex pheromone of the silk moth. Show how bombykol can be synthesized from the , example 2

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Chapter 11, Problem 43P

Chapter 11, Problem 45P

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Chapter 11 Solutions

Pearson eText Organic Chemistry -- Instant Access (Pearson+)

Ch. 11.1 - Prob. 1P Ch. 11.2 - Which is more reactive an organolithium compound...Ch. 11.2 - Prob. 3P Ch. 11.3 - Muscalure is the sex attractant of the common...Ch. 11.3 - Prob. 7P Ch. 11.3 - Prob. 8P Ch. 11.3 - Prob. 9P Ch. 11.3 - Prob. 10P Ch. 11.4 - Prob. 13P Ch. 11.4 - Prob. 14P

Ch. 11.4 - Prob. 15P Ch. 11.4 - Prob. 16P Ch. 11.4 - Prob. 17P Ch. 11.4 - Prob. 19P Ch. 11.4 - Show how the Suzuki and/or Heck reactions can be...Ch. 11.4 - Identify two pairs of an alkyl bromide and an...Ch. 11.5 - Prob. 22P Ch. 11.5 - Draw the product of ring-closing metathesis for...Ch. 11.5 - Prob. 25P Ch. 11.5 - Prob. 26P Ch. 11 - Prob. 27P Ch. 11 - Prob. 28P Ch. 11 - The coupling of an alkyne with an aryl halide in...Ch. 11 - Identify A through H.Ch. 11 - Using the given starting material, any necessary...Ch. 11 - What alkyl halide reacts with lithium...Ch. 11 - Prob. 33P Ch. 11 - Prob. 34P Ch. 11 - The following compound undergoes an intramolecular...Ch. 11 - Using ethynyleyclohexane as a starting material...Ch. 11 - Prob. 37P Ch. 11 - Using the given starting material, any necessary...Ch. 11 - Prob. 39P Ch. 11 - A student added an equivalent of...Ch. 11 - Using the given starting material, any necessary...Ch. 11 - Prob. 42P Ch. 11 - Prob. 43P Ch. 11 - Bombykol is the sex pheromone of the silk moth....Ch. 11 - Prob. 45P Ch. 11 - Prob. 46P Ch. 11 - A dibromide loses only one bromine when it reacts...Ch. 11 - What starting material is required in order to...Ch. 11 - What product is obtained from ring-opening...

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Bombykol is the sex pheromone of the silk moth. Show how bombykol can be synthesized from the following compounds.

Solution Summary: The author explains that Bombykol can be synthesized from the given compound by using Suzuki reaction and Heck reaction.

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Chapter 11 Solutions